Pyrazine

Details

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Internal ID 677aa85f-452d-42e7-8f82-28ba174793d7
Taxonomy Organoheterocyclic compounds > Diazines > Pyrazines
IUPAC Name pyrazine
SMILES (Canonical) C1=CN=CC=N1
SMILES (Isomeric) C1=CN=CC=N1
InChI InChI=1S/C4H4N2/c1-2-6-4-3-5-1/h1-4H
InChI Key KYQCOXFCLRTKLS-UHFFFAOYSA-N
Popularity 17,101 references in papers

Physical and Chemical Properties

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Molecular Formula C4H4N2
Molecular Weight 80.09 g/mol
Exact Mass 80.037448136 g/mol
Topological Polar Surface Area (TPSA) 25.80 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.48
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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290-37-9
1,4-Diazine
p-Diazine
Paradiazine
Piazine
1,4-Diazabenzene
pyrazin
CCRIS 1331
1,4-Diazin
EINECS 206-027-6
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pyrazine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9865 98.65%
Caco-2 + 0.8705 87.05%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Mitochondria 0.6651 66.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9796 97.96%
OATP1B3 inhibitior + 0.9624 96.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8859 88.59%
P-glycoprotein inhibitior - 0.9893 98.93%
P-glycoprotein substrate - 0.9957 99.57%
CYP3A4 substrate - 0.8812 88.12%
CYP2C9 substrate - 0.8019 80.19%
CYP2D6 substrate - 0.7743 77.43%
CYP3A4 inhibition - 0.7952 79.52%
CYP2C9 inhibition - 0.9532 95.32%
CYP2C19 inhibition - 0.9750 97.50%
CYP2D6 inhibition - 0.9358 93.58%
CYP1A2 inhibition - 0.5094 50.94%
CYP2C8 inhibition - 0.9719 97.19%
CYP inhibitory promiscuity - 0.7877 78.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5067 50.67%
Eye corrosion + 0.9292 92.92%
Eye irritation + 0.9956 99.56%
Skin irritation + 0.9434 94.34%
Skin corrosion + 0.8425 84.25%
Ames mutagenesis - 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7941 79.41%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation + 0.7104 71.04%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.4516 45.16%
Acute Oral Toxicity (c) II 0.4825 48.25%
Estrogen receptor binding - 0.9086 90.86%
Androgen receptor binding - 0.9204 92.04%
Thyroid receptor binding - 0.7879 78.79%
Glucocorticoid receptor binding - 0.8661 86.61%
Aromatase binding - 0.8801 88.01%
PPAR gamma - 0.8893 88.93%
Honey bee toxicity - 0.8315 83.15%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity - 0.8958 89.58%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
No predicted targets yet!

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Coffea arabica
Nelumbo nucifera
Perilla frutescens

Cross-Links

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PubChem 9261
NPASS NPC158948
LOTUS LTS0074122
wikiData Q424284